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Aesculap Inc recalls Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N
Recalled November 5, 2025 · FDA recall Z-0312-2026 · Aesculap
Hazard
It was determined there is the potential of silicone fragments detaching from the yellow sealing component. · FDA Class II
Units
155 units
Sold at
Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada.
Description
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Product
Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A Product Description: REDUCING CONVERTER 10/12MM TO 5MM Component: N/A
Manufacturer(s)
Aesculap Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →